IRCT2014050117387N2已完成未知
Compare the effects of reflexology and relaxation on physical and mental symptoms in women with multiple sclerosis
Research Deputy Isfahan University of Medical Sciences0 个研究点目标入组 75 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 75
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 50 years（—）
- 性别
- Female
入选标准
- •Inclusion criteria : Women aged 18-50 years suffering from MS (relapsing-remitting, primary progressive and secondary progressive); MS final diagnosis by neurologists based on McDonald criteria with the elapse of at least 6 months from relevant diagnosis; tendency to participate in the research; no previous participation at treatment sessions of complementary medicine methods such as reflexology, relaxation, massage for the last 6 months; to feel chronic pain in at least one body organs, previous use of pain medication and Numerical Rating Scale (NRS); having the fatigue severity score of equal to and over 4 based on fatigue severity scale( FSS); have high scores of depression (more than 13), anxiety (more than 9) and stress (more than 18) based on DASS-21 scale; acquisition of scores 0-5.5 based on the Expanded Disability Status Scale( EDSS); not being in the menstruation period, nonexistence of deformity, callus or corn in the feet, feet lesion or cleft, active thrombosis or phlebitis, Varicose veins, record of latest ankle trauma, sprain, fracture, feet palm inflammation or infection; no affliction with diseases other than MS such as febrile acute or bodily chronic (flu, cardiac disabling, glands, respiratory, hepatic, skeletomuscular, renal), mental or psychic disorders such as severe depression, speech or hearing disorder; no addiction to narcotics and psychotropic; not being a member to the treatment crew (physician, nurse); to feel chronic pain in at least one body organs; previous use of pain medication and Numerical Rating Scale (NRS) pain score more 4 for at least 6 months; no pregnancy or no willingness to be pregnant and after taking of informed written consent. Exclusion criteria: No wanting to continue cooperation in research, use another CAM either current; absence of more than two session's acute relapse of the disease one month preceding ordering the study period or within study
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研究者
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